Huang L Y, Ehrenstein G, Catterall W A
Biophys J. 1978 Aug;23(2):219-31. doi: 10.1016/S0006-3495(78)85444-7.
The neurotoxins, batrachotoxin and veratridine, are specific activators of sodium channels and cause an increase in the rate of 22Na uptake in neuroblastoma cells. Yohimbine, an indolakylamine alkaloid, inhibits this batrachotoxin-induced 22Na uptake. The dose-response curve of yohimbine suggest that the inhibitor acts reversibly on a single class of binding sites with dissociation constant of 3--4 x 10(-5) M. The dissociation constant is not affected by depolarization from--41 to 0 mV. Kinetic and equilibrium experiments indicate that yohimbine is a competitive inhibitor of the action of batrachotoxin. These results support the conclusion that yohimbine inhibitis the sodium flux by acting on the channel gating mechanism rather than by occluding the channels.
神经毒素、箭毒蛙毒素和藜芦碱是钠通道的特异性激活剂,可使神经母细胞瘤细胞中22Na摄取速率增加。育亨宾是一种吲哚烷基胺生物碱,可抑制箭毒蛙毒素诱导的22Na摄取。育亨宾的剂量反应曲线表明,该抑制剂对单一类结合位点起可逆作用,解离常数为3 - 4×10(-5)M。解离常数不受从-41 mV到0 mV去极化的影响。动力学和平衡实验表明,育亨宾是箭毒蛙毒素作用的竞争性抑制剂。这些结果支持以下结论:育亨宾通过作用于通道门控机制而非阻塞通道来抑制钠通量。